Variant report

Variant	nsv947897
Chromosome Location	chr10:44098895-44102321
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:795)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr10:44101682-44102124	K562	blood:	n/a	n/a
2	BCLAF1	chr10:44101688-44102046	GM12878	blood:	n/a	chr10:44101839-44101848 chr10:44101855-44101864
3	BCLAF1	chr10:44101644-44102012	GM12878	blood:	n/a	chr10:44101839-44101848 chr10:44101855-44101864
4	BCLAF1	chr10:44101638-44102151	K562	blood:	n/a	chr10:44101839-44101848 chr10:44101855-44101864
5	BHLHE40	chr10:44101706-44102019	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:44101415-44102130	K562	blood:	n/a	chr10:44102038-44102054
7	BRCA1	chr10:44101733-44102001	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr10:44101381-44102293	K562	blood:	n/a	n/a
9	CBX3	chr10:44101644-44102052	K562	blood:	n/a	n/a
10	CCNT2	chr10:44101814-44102278	K562	blood:	n/a	n/a
11	CEBPB	chr10:44100381-44100596	HepG2	liver:	n/a	chr10:44100431-44100442
12	CEBPB	chr10:44100406-44100595	K562	blood:	n/a	chr10:44100431-44100442
13	CEBPB	chr10:44102201-44102382	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr10:44100344-44100588	IMR90	lung:	n/a	chr10:44100431-44100442
15	CEBPB	chr10:44101663-44102290	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr10:44100330-44100587	A549	lung:	n/a	chr10:44100431-44100442
17	CEBPD	chr10:44101756-44102110	HepG2	liver:	n/a	n/a
18	CHD2	chr10:44101488-44102042	GM12878	blood:	n/a	n/a
19	CHD2	chr10:44101610-44102069	K562	blood:	n/a	n/a
20	CHD2	chr10:44101880-44102041	HepG2	liver:	n/a	n/a
21	CHD2	chr10:44101657-44102469	Hela-S3	cervix:	n/a	chr10:44102080-44102090
22	CHD2	chr10:44101714-44102063	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr10:44101657-44102095	A549	lung:	n/a	n/a
24	CTCF	chr10:44101900-44102050	HUVEC	blood vessel:	n/a	chr10:44102039-44102048
25	CTCF	chr10:44101780-44101930	Caco-2	colon:	n/a	n/a
26	CTCF	chr10:44101733-44102012	K562	blood:	n/a	n/a
27	CTCF	chr10:44101790-44102004	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr10:44101500-44101650	GM12864	blood:	n/a	n/a
29	CTCF	chr10:44101580-44101730	MCF-7	breast:	n/a	n/a
30	CTCF	chr10:44101820-44101970	AG04449	skin:	n/a	n/a
31	CTCF	chr10:44101660-44101810	HFF	foreskin:	n/a	n/a
32	CTCF	chr10:44101680-44101830	GM12873	blood:	n/a	n/a
33	CTCF	chr10:44101720-44101870	BJ	skin:	n/a	n/a
34	CTCF	chr10:44101740-44101890	Caco-2	colon:	n/a	n/a
35	CTCF	chr10:44101850-44101967	GM19238	blood:	n/a	n/a
36	CTCF	chr10:44101400-44101550	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr10:44101840-44101990	NHLF	lung:	n/a	n/a
38	CTCF	chr10:44101560-44101710	K562	blood:	n/a	n/a
39	CTCF	chr10:44101740-44101890	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr10:44101560-44101710	MCF-7	breast:	n/a	n/a
41	CTCF	chr10:44101520-44101670	BJ	skin:	n/a	n/a
42	CTCF	chr10:44101840-44101990	SAEC	small airway:	n/a	n/a
43	CTCF	chr10:44101600-44101750	AG09309	skin:	n/a	n/a
44	CTCF	chr10:44101540-44101690	HPF	lung:	n/a	n/a
45	CTCF	chr10:44101580-44101730	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr10:44101680-44101830	HMF	breast:	n/a	n/a
47	CTCF	chr10:44101600-44101750	WI-38	lung:	n/a	n/a
48	CTCF	chr10:44101480-44101630	HPF	lung:	n/a	n/a
49	CTCF	chr10:44101840-44101990	GM12871	blood:	n/a	n/a
50	CTCF	chr10:44101620-44101770	HPAF	blood vessel:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:44102227-44102277	Hepatocyte	liver:	n/a
2	chr10:44101962-44102012	NHDF-neo	bronchial:	n/a
3	chr10:44102227-44102277	Hepatocyte	liver:	n/a
4	chr10:44101962-44102012	NHDF-neo	bronchial:	n/a
5	chr10:44101814-44101864	PrEC	prostate:	n/a
6	chr10:44101789-44101839	ECC-1	luminal epithelium:	n/a
7	chr10:44102035-44102085	LNCaP	prostate:	n/a
8	chr10:44101814-44101864	BJ	skin:	n/a
9	chr10:44102035-44102085	AG04450	lung:	fetal
10	chr10:44101814-44101864	U87	brain:	n/a
11	chr10:44101962-44102012	SK-N-MC	brain:	n/a
12	chr10:44101962-44102012	GM19239	blood:	n/a
13	chr10:44102227-44102277	GM19239	blood:	n/a
14	chr10:44101845-44101895	HAEpiC	amniotic membrane:	n/a
15	chr10:44102227-44102277	HCF	heart:	n/a
16	chr10:44101496-44101546	AG04449	skin:	fetal
17	chr10:44101814-44101864	CMK	blood:	n/a
18	chr10:44102035-44102085	HCF	heart:	n/a
19	chr10:44101728-44101778	AG04449	skin:	fetal
20	chr10:44101728-44101778	HCT-116	colon:	n/a
21	chr10:44101728-44101778	ovcar-3	ovarian:	n/a
22	chr10:44101789-44101839	LNCaP	prostate:	n/a
23	chr10:44101569-44101619	GM12891	blood:	n/a
24	chr10:44101814-44101864	GM12891	blood:	n/a
25	chr10:44101496-44101546	Hela-S3	cervix:	n/a
26	chr10:44101845-44101895	HEEpiC	esophagus:	n/a
27	chr10:44099144-44099194	AG04449	skin:	fetal
28	chr10:44101714-44101764	K562	blood:	n/a
29	chr10:44102227-44102277	AoSMC	blood vessel:	n/a
30	chr10:44101496-44101546	SK-N-SH	brain:	n/a
31	chr10:44101814-44101864	HIPEpiC	eye:	n/a
32	chr10:44101569-44101619	H1-hESC	embryonic stem cell:	embryo
33	chr10:44101962-44102012	K562	blood:	n/a
34	chr10:44101728-44101778	T-47D	breast:	n/a
35	chr10:44099144-44099194	ProgFib	skin:	n/a
36	chr10:44102227-44102277	HPAEpiC	pulmonary alveolar:	n/a
37	chr10:44099144-44099194	SKMC	muscle:	n/a
38	chr10:44099144-44099194	GM12878	blood:	n/a
39	chr10:44101728-44101778	SK-N-SH_RA	brain:	n/a
40	chr10:44101814-44101864	SK-N-SH_RA	brain:	n/a
41	chr10:44101720-44101770	ProgFib	skin:	n/a
42	chr10:44101569-44101619	GM12892	blood:	n/a
43	chr10:44101720-44101770	Jurkat	blood:	n/a
44	chr10:44101720-44101770	PANC-1	pancreas:	n/a
45	chr10:44101789-44101839	ovcar-3	ovarian:	n/a
46	chr10:44102035-44102085	SK-N-SH_RA	brain:	n/a
47	chr10:44101569-44101619	PANC-1	pancreas:	n/a
48	chr10:44101814-44101864	GM12892	blood:	n/a
49	chr10:44101496-44101546	GM06990	blood:	n/a
50	chr10:44101845-44101895	Caco-2	colon:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:43902834..43905281-chr10:44101183..44103050,2	MCF-7	breast:
2	chr10:44100401..44102576-chr10:44125762..44128541,3	MCF-7	breast:
3	chr10:44068620..44071892-chr10:44099602..44104778,6	MCF-7	breast:
4	chr10:44090591..44094323-chr10:44095437..44099024,4	K562	blood:
5	chr10:44100612..44103408-chr10:44143126..44145241,3	MCF-7	breast:
6	chr10:44101689..44104570-chr10:44142385..44144867,2	K562	blood:
7	chr10:43901770..43904893-chr10:44100789..44103373,5	MCF-7	breast:
8	chr10:44101948..44103736-chr10:44112842..44114358,2	MCF-7	breast:
9	chr10:44097620..44100103-chr10:44100375..44102057,3	K562	blood:
10	chr10:43891174..43892847-chr10:44101479..44103589,2	K562	blood:
11	chr10:44068669..44071698-chr10:44096672..44099575,3	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF487P-7	chr10:44101867-44101994	NONHSAT012974

No data

Variant related genes	Relation type
ZNF485	TF binding region
CAP1P2	TF binding region
ZNF485	CpG island
CAP1P2	CpG island
ENSG00000198298	chromatin interactions
ENSG00000169740	chromatin interactions
ENSG00000238263	chromatin interactions
ENSG00000196793	chromatin interactions
ENSG00000237389	chromatin interactions
ENSG00000232004	chromatin interactions
ENSG00000169813	chromatin interactions

Extended variants
information (count: 128 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:128 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570994509	chr10:44098904-44098905	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs7096121	chr10:44098964-44098965	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs111822047	chr10:44099012-44099013	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs192513077	chr10:44099126-44099127	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs574851862	chr10:44099131-44099132	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs535859630	chr10:44099141-44099142	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs143911709	chr10:44099144-44099145	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs569894621	chr10:44099148-44099149	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs143012459	chr10:44099157-44099158	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs78970962	chr10:44099160-44099161	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs540034985	chr10:44099190-44099191	Weak transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs73254871	chr10:44099201-44099202	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs570254061	chr10:44099216-44099217	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs565667390	chr10:44099217-44099218	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs369757060	chr10:44099224-44099225	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs577415292	chr10:44099273-44099274	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs544673451	chr10:44099286-44099287	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs2066046	chr10:44099347-44099348	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs117294859	chr10:44099355-44099356	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs548586665	chr10:44099361-44099362	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs560603131	chr10:44099362-44099363	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs111244154	chr10:44099364-44099365	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs576326022	chr10:44099366-44099367	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs189420244	chr10:44099377-44099378	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs192948748	chr10:44099400-44099401	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs2066045	chr10:44099408-44099409	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs550225443	chr10:44099429-44099430	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs568632615	chr10:44099439-44099440	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs535848324	chr10:44099462-44099463	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs554581090	chr10:44099504-44099505	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs532437999	chr10:44099520-44099521	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs574118863	chr10:44099536-44099537	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs534145851	chr10:44099547-44099548	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs11238597	chr10:44099571-44099572	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs74695962	chr10:44099616-44099617	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs75243662	chr10:44099617-44099618	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs577073366	chr10:44099654-44099655	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs1974282	chr10:44099665-44099666	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs141238043	chr10:44099699-44099700	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs11238598	chr10:44099754-44099755	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs552044257	chr10:44099779-44099780	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs367730462	chr10:44099800-44099801	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs372583350	chr10:44099827-44099828	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs184245694	chr10:44099881-44099882	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs551990446	chr10:44099898-44099899	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs116034454	chr10:44099940-44099941	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs563229031	chr10:44099948-44099949	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs564454137	chr10:44099955-44099956	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs531760472	chr10:44100009-44100010	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs189054190	chr10:44100015-44100016	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44091400-44101400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr10:44091800-44101200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr10:44092200-44101400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr10:44093000-44101600	Weak transcription	Primary T cells from cord blood	blood
5	chr10:44095000-44101400	Weak transcription	Spleen	Spleen
6	chr10:44098200-44101400	Weak transcription	Gastric	stomach
7	chr10:44100400-44101200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr10:44101200-44101400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr10:44101200-44101400	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr10:44101200-44101400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr10:44101200-44101400	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr10:44101200-44101400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr10:44101200-44101400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr10:44101200-44101400	Enhancers	Adipose Nuclei	Adipose
15	chr10:44101200-44101400	Enhancers	Brain Anterior Caudate	brain
16	chr10:44101200-44101400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr10:44101200-44101400	Enhancers	Ovary	ovary
18	chr10:44101200-44101400	Active TSS	Skeletal Muscle Male	skeletal muscle
19	chr10:44101200-44101400	Active TSS	Stomach Smooth Muscle	stomach
20	chr10:44101200-44101400	Enhancers	Dnd41	blood
21	chr10:44101200-44101400	Enhancers	NHDF-Ad	bronchial
22	chr10:44101200-44101600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr10:44101200-44101600	Enhancers	Right Ventricle	heart
24	chr10:44101200-44101800	Enhancers	Placenta Amnion	Placenta Amnion
25	chr10:44101200-44102200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr10:44101200-44102600	Active TSS	Brain Cingulate Gyrus	brain
27	chr10:44101200-44102600	Active TSS	Colon Smooth Muscle	Colon
28	chr10:44101200-44102800	Enhancers	Fetal Heart	heart
29	chr10:44101200-44103000	Active TSS	Brain Angular Gyrus	brain
30	chr10:44101400-44101600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr10:44101400-44101600	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr10:44101400-44101600	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr10:44101400-44101600	Enhancers	Primary B cells from peripheral blood	blood
34	chr10:44101400-44101600	Enhancers	Primary T cells fromperipheralblood	blood
35	chr10:44101400-44101600	Enhancers	Primary hematopoietic stem cells	blood
36	chr10:44101400-44101600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr10:44101400-44101600	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr10:44101400-44101600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr10:44101400-44101600	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr10:44101400-44101600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr10:44101400-44101600	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr10:44101400-44101600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr10:44101400-44101600	Enhancers	Liver	Liver
44	chr10:44101400-44101600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr10:44101400-44101600	Enhancers	Placenta	Placenta
46	chr10:44101400-44101600	Enhancers	Left Ventricle	heart
47	chr10:44101400-44101600	Enhancers	Pancreas	Pancrea
48	chr10:44101400-44101600	Enhancers	Psoas Muscle	Psoas
49	chr10:44101400-44101600	Enhancers	Right Atrium	heart
50	chr10:44101400-44101600	Enhancers	HMEC	breast

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